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Microfluidic Technology Applied to Protein Sizing and Quantitation

机译:微流技术应用于蛋白质定量和定量

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摘要

The current standard method for analyzing proteins is denaturing gel electrophoresis (SDS-PAGE). Researchers rely on this traditional method that has not substantially changed in the past 30 years. There is, however, a strong demand for automation and higher throughput. The development of microfluidics offers an alternative for protein analysis. The first commercial microfluidic system, the Agilent 2100 bioanalyzer, allows for rapid and automated separation of proteins. The chip-based protein analysis is comparable in sensitivity, sizing accuracy and reproducibility to SDS-PAGE stained with Coomassie. Resolution and linear dynamic range are improved. Absolute quantitation accuracy and reproducibility is superior to SDS-PAGE and is comparable to Lowry or Bradford. Agilent 2100 bioanalyzer offers significant advantages to SDS-PAGE such as: fast analysis times, ease of use, automated data analysis, and good reproducibility.
机译:当前用于分析蛋白质的标准方法是变性凝胶电泳(SDS-PAGE)。研究人员依靠的是这种传统方法,该方法在过去30年中没有发生太大变化。但是,对自动化和更高的吞吐量有强烈的需求。微流体技术的发展为蛋白质分析提供了另一种选择。第一个商业化的微流体系统,Agilent 2100生物分析仪,可以快速,自动地分离蛋白质。基于芯片的蛋白质分析在灵敏度,上浆精度和重现性方面与考马斯染色的SDS-PAGE相当。分辨率和线性动态范围得到改善。绝对定量准确度和重现性优于SDS-PAGE,可与Lowry或Bradford媲美。 Agilent 2100生物分析仪具有SDS-PAGE的显着优势,例如:分析时间短,易于使用,自动数据分析和良好的重现性。

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